Ethylene (CH) is one of the most significant substances in the petrochemical industry; however, the capture of acetylene (CH) in about 1% from CH/CH mixtures is a difficult task because of the similarity of their physical properties. With the aggravation of the energy crisis, using metal-organic framework (MOF) materials to purify CH through adsorptive separation is a promising way to save energy and reduce emission. Pore-space partition (PSP) with the aim of enhancing the density of the binding sites and the strength of the host-guest interactions is an effective means to promote a solution for the challenging gas separation problems. Herein, we report a new embedding metal-carboxylate chain-induced topology upgrade strategy within a MOF to realize PSP and separation of CH/CH mixtures. As a proof of concept, we construct a microporous MOF () utilizing the in situ insertion of cobalt terephthalic chains into a pretargeted ant-type framework during synthesis. Because of the attainment of an elaborately tuned aperture size and a specific pore environment through this strategy, (activated ) not only has a remarkable gas sorption capacity and strong interactions for CH but also possesses an excellent purification performance for CH/CH mixtures. Both experiments and simulation calculations clearly reveal that is a promising candidate for the separation of CH/CH, proving the feasibility of this new strategy for developing newly fashioned MOFs with adjustable structure and performance.
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http://dx.doi.org/10.1021/acs.inorgchem.1c03148 | DOI Listing |
Phys Chem Chem Phys
August 2024
Univ Rennes, CNRS, IPR (Institut de Physique de Rennes), UMR 6251, F-35000 Rennes, France.
CH was the first molecular ion identified in the interstellar medium and is found to be ubiquitous in interstellar clouds. However, its formation and destruction paths are not well understood, especially at low temperatures. A new theoretical approach based on the canonical variational transition state theory was used to study the H + CH reactive collisions.
View Article and Find Full Text PDFBiochemistry (Mosc)
December 2023
Faculty of Chemistry, Lomonosov Moscow State University, Moscow, 119991, Russia.
The study of many membrane enzymes in an aqueous medium is difficult due to the loss of their catalytic activity, which makes it necessary to use membrane-like systems, such as reverse micelles of surfactants in nonpolar organic solvents. However, it should be taken into account that the micelles are a simplified model of natural membranes, since membranes contain many different components, a significant part of which are phospholipids. In this work, we studied impact of the main phospholipids, phosphatidylcholine (PC) and phosphatidylethanolamine (PE), on activity of the membrane enzymes using galactonolactone oxidase from Trypanosoma cruzi (TcGAL) and L-galactono-1,4-lactone dehydrogenase from Arabidopsis thaliana (AtGALDH) as examples.
View Article and Find Full Text PDFInorg Chem
November 2023
Department of Chemistry, Indian Institute of Science Education and Research, Pune, Dr. Homi Bhabha Road, Pune 411008, India.
Chiral coordination cages have emerged as an efficient platform for enantioselective processes via host-guest interactions. Here, we report an enantiomeric pair of tetrahedral cages of formula [(Pd[PO(N(*CH(CH)Ph)])(CO)] supported by chiral tris(imido)phosphate trianions and squarate (CO) linkers. These cages exhibit unusual coordination isomerism for Pd(II)-linker bonds compared with the other Pd(II) cages of this family.
View Article and Find Full Text PDFAdv Colloid Interface Sci
November 2023
University of Ulm, D-89081 Ulm, Germany.
The monolayer characteristics of selected N-alkanoyl substituted α-amino acid are studied with the objective to demonstrate the specific effect of the chemical structure of the polar head group which is highlighted with the D- and L-enantiomers of the following selected examples: R-alanine, R-serine, R-threonine, R-allo-threonine, and R-aspartic acid (R = C, C). The thermodynamic effect of the head group variation is studied. Experimental π-A isotherms of the N-tetradecyl-L-alanine monolayers show similar behavior as those of usual amphiphiles.
View Article and Find Full Text PDFOrganometallics
July 2023
Department of Chemistry, University of California, 1 Shields Avenue, Davis, California 95616, United States.
Two compounds containing a Sn(II) atom supported by a bidentate biscarborane ligand have been synthesized via salt metathesis. The synthetic procedures for ()Sn·THF ( = 1,1' (-carborane) () and K[()Sn] () involved the reaction of K[] with SnCl in either a THF solution () or in a benzene/dichloromethane solvent mixture (). Using the same solvent conditions as those used for but using a shorter reaction time gave a dibiscarboranyl ethene ().
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